Derrone

Modify Date: 2025-08-25 11:24:00

Derrone Structure
Derrone structure
Common Name Derrone
CAS Number 76166-59-1 Molecular Weight 336.34
Density 1.4±0.1 g/cm3 Boiling Point 584.1±50.0 °C at 760 mmHg
Molecular Formula C20H16O5 Melting Point N/A
MSDS N/A Flash Point 214.6±23.6 °C

 Use of Derrone


Derrone, a prenylated isoflavones, is an Aurora kinase inhibitor, with IC50 values of 6 and 22.3 μM against Aurora B and Aurora A, respectively. Derrone shows anti-tumor activity[1][2].

 Names

Name Derrone
Synonym More Synonyms

 Derrone Biological Activity

Description Derrone, a prenylated isoflavones, is an Aurora kinase inhibitor, with IC50 values of 6 and 22.3 μM against Aurora B and Aurora A, respectively. Derrone shows anti-tumor activity[1][2].
Related Catalog
Target

IC50: 6 μM (Aurora kinase B), 22.3 μM (Aurora kinase A)[1]

In Vitro Derrone (30-60 μM, 15 days) significantly inhibits the formation and growth of MCF7 tumor spheroids, with the tumor spheroid growth inhibition (% TGI) of 17.5% and 65.4% for 30 and 60 μM Derrone, respectively[1]. Derrone shows the autophagic features, such as the conversion of LC3-I to LC3-II, the formation of autophagosome and the downregulation of SQSTM1/p62 (p62)[2]. Derrone induces autophagic cell death through intracellular ROS and sustained ERK phosphorylation in A549 cells[2].
References

[1]. Hoang NT, et al. In Vitro Characterization of Derrone as an Aurora Kinase Inhibitor. Biol Pharm Bull. 2016 Jun 1;39(6):935-45.

[2]. Kang MJ, et al. Derrone induces autophagic cell death through induction of ROS and ERK in A549 cells. PLoS One. 2019 Jun 19;14(6):e0218659.

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Boiling Point 584.1±50.0 °C at 760 mmHg
Molecular Formula C20H16O5
Molecular Weight 336.34
Flash Point 214.6±23.6 °C
Exact Mass 336.099762
PSA 79.90000
LogP 5.53
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.660
InChIKey ZSYPWSSGRVZENH-UHFFFAOYSA-N
SMILES CC1(C)C=Cc2c(cc(O)c3c(=O)c(-c4ccc(O)cc4)coc23)O1

 Safety Information

Hazard Codes Xi

 DerroneBioassay

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Name: Antiproliferative activity against human SW480 cells at 10 uM after 24 hrs by MTS ass...
Source: ChEMBL
Target: SW480
External Id: CHEMBL4053426
Name: HIV Enzyme Data
Source: NIAID
Target: N/A
External Id: HIV Enzyme Data
Name: Antiproliferative activity against human U937 cells after 48 hrs by WST-8 assay
Source: ChEMBL
Target: U-937
External Id: CHEMBL885742
Name: Activation of Nrf2 (unknown origin) expressed in human HepG2 cells at 10 uM after 6 h...
Source: ChEMBL
Target: Nuclear factor erythroid 2-related factor 2
External Id: CHEMBL4053417
Name: Antiproliferative activity against human U937 cells after 72 hrs by WST-8 assay
Source: ChEMBL
Target: U-937
External Id: CHEMBL885743
Name: Inhibition of recombinant human PTP1B using pNPP as substrate at 10 uM after 30 mins ...
Source: ChEMBL
Target: Tyrosine-protein phosphatase non-receptor type 1
External Id: CHEMBL4053415
Name: Inhibition of tyrosinase (unknown origin) using L-tyrosine as substrate at 10 uM prei...
Source: ChEMBL
Target: Tyrosinase
External Id: CHEMBL4053412
Name: Antiproliferative activity against human U937 cells after 24 hrs by WST-8 assay
Source: ChEMBL
Target: U-937
External Id: CHEMBL885741
Name: Antiproliferative activity against human A549 cells at 10 uM after 24 hrs by MTS assa...
Source: ChEMBL
Target: A549
External Id: CHEMBL4053424
Name: Antiproliferative activity against human MCF7 cells at 10 uM after 24 hrs by MTS assa...
Source: ChEMBL
Target: MCF7
External Id: CHEMBL4053425
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 Synonyms

5-Hydroxy-3-(4-hydroxyphenyl)-8,8-dimethyl-4H,8H-pyrano[2,3-f]chromen-4-one
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